Canonical Allele Identifier: CA4701547

Gene: GSR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30709923_30709924del , CM000670.2:g.30709923_30709924del	GRCh38
NC_000008.10:g.30567440_30567441del , CM000670.1:g.30567440_30567441del	GRCh37
NC_000008.9:g.30686982_30686983del	NCBI36
NG_027719.1:g.23062_23063del

Transcript Alleles

HGVS	Amino-acid Change
NM_000637.5:c.334-6_334-5del MANE Select	NP_000628.2:n.334-6_334-5del
ENST00000221130.11:c.334-6_334-5del MANE Select	ENSP00000221130.5:n.334-6_334-5del
NM_000637.3:c.334-6_334-5del	NP_000628.2:n.334-6_334-5del
NM_000637.4:c.334-6_334-5del	NP_000628.2:n.334-6_334-5del
NM_001195102.1:c.334-6_334-5del	NP_001182031.1:n.334-6_334-5del
NM_001195102.2:c.334-6_334-5del	NP_001182031.1:n.334-6_334-5del
NM_001195102.3:c.334-6_334-5del	NP_001182031.1:n.334-6_334-5del
NM_001195103.1:c.334-6_334-5del	NP_001182032.1:n.334-6_334-5del
NM_001195103.2:c.334-6_334-5del	NP_001182032.1:n.334-6_334-5del
NM_001195103.3:c.334-6_334-5del	NP_001182032.1:n.334-6_334-5del
NM_001195104.1:c.334-6_334-5del	NP_001182033.1:n.334-6_334-5del
NM_001195104.2:c.334-6_334-5del	NP_001182033.1:n.334-6_334-5del
NM_001195104.3:c.334-6_334-5del	NP_001182033.1:n.334-6_334-5del
ENST00000221130.9:c.334-6_334-5del	ENSP00000221130.5:n.334-6_334-5del
ENST00000521479.1:c.-3-6_-3-5del	ENSP00000430825.1:n.-3-6_-3-5del
ENST00000523295.5:c.166-6_166-5del	ENSP00000431044.1:n.166-6_166-5del
ENST00000537535.5:c.334-6_334-5del	ENSP00000438845.1:n.334-6_334-5del
ENST00000541648.5:c.334-6_334-5del	ENSP00000444559.1:n.334-6_334-5del
ENST00000546342.5:c.334-6_334-5del	ENSP00000445516.1:n.334-6_334-5del
ENST00000643525.1:n.81-6_81-5del
ENST00000643653.1:c.200-6_200-5del